India's DMPLOI - Jobs & Networking AppCORONA Remedies Limited, one of India’s fastest-growing pharmaceutical companies headquartered in Ahmedabad, has announced a Walk-In Interview for experienced professionals in Production, Quality Assurance (QA), Quality Control (QC), Microbiology, and Engineering departments. Candidates with relevant pharmaceutical manufacturing experience are invited to attend the interview on 5th July 2026 (Sunday).
If you have experience in OSD (Oral Solid Dosage) manufacturing, IPQA, QMS, Quality Control, Microbiology, or Engineering Maintenance, this is an excellent opportunity to join a rapidly expanding pharmaceutical organization.
Company Overview
Company Name: CORONA Remedies Limited
Industry: Pharmaceutical Manufacturing
Head Office: Ahmedabad, Gujarat, India
CORONA Remedies Limited is recognized for its employee-focused work culture and continuous growth in the pharmaceutical sector. The company has over 5,000 employees and continues to expand its manufacturing operations.
Walk-In Interview Details
Interview Date: 5th July 2026 (Sunday)
Time: 9:30 AM to 2:00 PM
Interview Venue
CORONA Remedies Limited
Block S, Mondeal Business Park, Near Gurudwara,
S.G. Highway, Ahmedabad, Gujarat
Job Location
CORONA Remedies Limited
Near Super Gas Pump, Bavla Bagodara Road,
Village: Bhayla, Taluka: Bavla,
District: Ahmedabad, Gujarat
Department-wise Vacancies
1. Production
Designation
Sr. Officer / Executive
Operator
Qualification
B.Pharm (Sr. Officer/Executive)
ITI (Operator)
Experience
3–8 Years
Required Skills
Exposure to OSD Manufacturing
Granulation
Compression
Coating
Packing
Operation of manufacturing equipment
2. Quality Assurance (QA)
Designation
Sr. Officer / Executive – IPQA
Executive – QMS
Qualification
B.Pharm / M.Sc.
Experience
IPQA: 2–8 Years
QMS: 4–6 Years
Required Skills
IPQA activities
OSD Manufacturing
Change Control
Deviation Handling
CAPA
Vendor Qualification
GMP Documentation
3. Quality Control (QC)
Designation
Sr. Officer / Executive
Sr. Officer / Executive (Micro)
Qualification
B.Pharm / M.Sc.
M.Sc. (Microbiology)
Experience
QC Executive: 3–8 Years
Microbiology: 4–6 Years
Required Skills
HPLC
Dissolution Testing
Disintegration Test Apparatus
FTIR
UV Spectrophotometer
Weighing Balance
Friability Tester
Hardness Tester
Raw Material Analysis
In-process Testing
Finished Product Analysis
Stability Studies
Process Validation
Analytical Deviation
OOS/OOT Investigation
Environmental Monitoring
Water Testing
SOP & GMP Compliance
4. Engineering
Designation
Officer / Senior Officer
Qualification
BE / Diploma (Mechanical or Electrical)
Experience
2–6 Years
Required Skills
Preventive Maintenance
Predictive Maintenance
Breakdown Maintenance
HVAC
AHU
Chillers
Air Compressors
Boilers
DG Sets
Water Systems
Utility Equipment
GMP Compliance
Engineering SOPs
Safety Procedures
Eligibility Criteria
Relevant pharmaceutical manufacturing experience.
Experience in OSD manufacturing is preferred for Production and QA roles.
Candidates should have good knowledge of GMP, SOPs, documentation, and regulatory compliance.
Unable to Attend the Walk-In?
Candidates who cannot attend the interview on 5th July 2026 can send their updated CV to:
anjaliv@coronaremedies.com
sagart@coronaremedies.com
Why Join CORONA Remedies?
Fast-growing pharmaceutical company
Excellent employee work culture
Career growth opportunities
Modern manufacturing facility
Exposure to regulated pharmaceutical operations
Learning-oriented environment
Documents to Carry
Updated Resume
Recent Passport Size Photographs
Educational Certificates
Experience Certificates
Latest Salary Slips
Identity Proof (Aadhaar/PAN)
Passport (if available)
Technical FAQs
1. What is IPQA in pharmaceutical manufacturing?
IPQA (In-Process Quality Assurance) ensures manufacturing activities comply with GMP during production through line clearance, process monitoring, sampling, and documentation.
2. What instruments should a QC analyst be familiar with?
A QC analyst should have practical knowledge of HPLC, FTIR, UV-Visible Spectrophotometer, Dissolution Tester, Disintegration Tester, Friability Tester, Hardness Tester, and analytical balances.
3. What is CAPA in Quality Assurance?
CAPA (Corrective and Preventive Action) is a quality system used to investigate deviations, identify root causes, implement corrective actions, and prevent recurrence.
4. What are OOS and OOT investigations?
OOS (Out of Specification) refers to test results outside established specifications, while OOT (Out of Trend) indicates unexpected analytical trends. Both require documented investigation as per GMP guidelines.
5. What are the responsibilities of an Engineering Officer in a pharmaceutical plant?
Engineering Officers maintain production and utility equipment, including HVAC, AHU, boilers, chillers, DG sets, air compressors, and water systems, ensuring equipment reliability, GMP compliance, and uninterrupted production.
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